F. Ajmar

945 total citations
56 papers, 748 citations indexed

About

F. Ajmar is a scholar working on Hematology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, F. Ajmar has authored 56 papers receiving a total of 748 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Hematology, 17 papers in Cellular and Molecular Neuroscience and 13 papers in Molecular Biology. Recurrent topics in F. Ajmar's work include Chronic Myeloid Leukemia Treatments (13 papers), Acute Myeloid Leukemia Research (11 papers) and Hereditary Neurological Disorders (8 papers). F. Ajmar is often cited by papers focused on Chronic Myeloid Leukemia Treatments (13 papers), Acute Myeloid Leukemia Research (11 papers) and Hereditary Neurological Disorders (8 papers). F. Ajmar collaborates with scholars based in Italy, United States and Switzerland. F. Ajmar's co-authors include Paola Mandich, Emilia Bellone, Mario Sessarego, Emilio Di Maria, Roberto Ravazzolo, E Salvidio, Cecilia Garrè, Domenico Coviello, Raffaella Defferrari and Gianluigi Mancardi and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Neurology.

In The Last Decade

F. Ajmar

54 papers receiving 720 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
F. Ajmar Italy 17 253 249 209 189 163 56 748
Franco Ajmar Italy 19 371 1.5× 235 0.9× 118 0.6× 119 0.6× 341 2.1× 46 1.0k
Anna Migdalska‐Richards United Kingdom 11 190 0.8× 131 0.5× 125 0.6× 53 0.3× 492 3.0× 19 1.0k
S Parmentier France 10 164 0.6× 160 0.6× 149 0.7× 29 0.2× 107 0.7× 15 588
Anita E. Harding United Kingdom 13 419 1.7× 297 1.2× 18 0.1× 60 0.3× 145 0.9× 15 710
Josef Ekstein United States 12 407 1.6× 170 0.7× 20 0.1× 64 0.3× 48 0.3× 27 851
Martin Horan Australia 14 375 1.5× 51 0.2× 33 0.2× 32 0.2× 173 1.1× 24 797
Manuèle Miné France 17 362 1.4× 34 0.1× 36 0.2× 29 0.2× 150 0.9× 27 612
Keiko Miyake Japan 13 201 0.8× 83 0.3× 23 0.1× 31 0.2× 46 0.3× 30 755
J. Bardakdjian France 13 134 0.5× 111 0.4× 193 0.9× 305 1.6× 22 0.1× 40 551
Bernhard Weschke Germany 13 547 2.2× 116 0.5× 23 0.1× 29 0.2× 96 0.6× 23 985

Countries citing papers authored by F. Ajmar

Since Specialization
Citations

This map shows the geographic impact of F. Ajmar's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by F. Ajmar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F. Ajmar more than expected).

Fields of papers citing papers by F. Ajmar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F. Ajmar. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by F. Ajmar. The network helps show where F. Ajmar may publish in the future.

Co-authorship network of co-authors of F. Ajmar

This figure shows the co-authorship network connecting the top 25 collaborators of F. Ajmar. A scholar is included among the top collaborators of F. Ajmar based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with F. Ajmar. F. Ajmar is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Trakalo, Joseph, Tasha Cate‐Carter, F. Ajmar, et al.. (2003). Glutamate receptor gene (GRIN1, GRIN2B) in schizophrenia: TDT and case-controls analyses. Schizophrenia Research. 60(1). 85–85. 1 indexed citations
2.
Abbruzzese, Genevieve, Emilio Di Maria, Paolo Martinelli, et al.. (2001). Clinical and genetic study of essential tremor in the Italian population. Neurological Sciences. 22(1). 39–40. 25 indexed citations
3.
Maria, Emilio Di, Roberta Marchese, Andrea Assini, et al.. (2001). No evidence of association between CAG expansions and essential tremor in a large cohort of Italian patients. Journal of Neural Transmission. 108(3). 297–304. 11 indexed citations
4.
Mandich, Paola, Gianluigi Mancardi, Emilio Di Maria, et al.. (1999). Congenital hypomyelination due to myelin protein zero Q215X mutation. Annals of Neurology. 45(5). 676–678. 35 indexed citations
5.
Mandich, Paola, Gioia Jacopini, Emilio Di Maria, et al.. (1998). Predictive testing for Huntington’s disease: ten years’ experience in two Italian centres. The Italian Journal of Neurological Sciences. 19(2). 68–74. 20 indexed citations
6.
Schito, Anna Maria, Antonio Pizzuti, Emilio Di Maria, et al.. (1997). mRNA distribution in adult human brain of GRIN2B, a N-methyl-d-aspartate (NMDA) receptor subunit. Neuroscience Letters. 239(1). 49–53. 37 indexed citations
7.
Mandich, Paola, Emilio Di Maria, Emilia Bellone, F. Ajmar, & Giovanni Abbruzzese. (1996). Molecular Analysis of the IT15 Gene in Patients with Apparently ‘Sporadic’ Huntington’s Disease. European Neurology. 36(6). 348–352. 4 indexed citations
8.
Mancardi, Gianluigi, Paola Mandich, Angelo Schenone, et al.. (1995). Progressive sensory-motor polyneuropathy with tomaculous changes is associated to 17p11.2 deletion. Journal of the Neurological Sciences. 131(1). 30–34. 21 indexed citations
9.
Mancardi, Gianluigi, Antonio Uccelli, Emilia Bellone, et al.. (1994). 17p11.2 Duplication Is a Common Finding in Sporadic Cases of Charcot-Marie-Tooth Type 1. European Neurology. 34(3). 135–139. 6 indexed citations
10.
Novelletto, Andrea, Francesca Persichetti, Paola Mandich, et al.. (1994). Analysis of the trinucleotide repeat expansion in Italian families affected with Huntington disease. Human Molecular Genetics. 3(1). 93–98. 46 indexed citations
11.
Sessarego, Mario, et al.. (1991). Involvement of the short arm of the derivative chromosome 9 in Philadelphia-positive acute lymphoblastic leukemia. Cancer Genetics and Cytogenetics. 52(1). 43–49. 9 indexed citations
12.
Gasparini, Paolo, Paola Mandich, Giuseppe Novelli, et al.. (1991). Forensic Applications of Molecular Genetic Analysis: An Italian Collaborative Study on Paternity Testing by the Determination of Variable Number of Tandem Repeat DNA Polymorphisms. Human Heredity. 41(3). 174–181. 30 indexed citations
13.
Mandich, Paola, Gabriella Restagno, Giuseppe Novelli, et al.. (1990). Autosomal dominant Polycystic Kidney Disease: A linkage evaluation of heterogeneity in Italy. American Journal of Medical Genetics. 35(4). 579–581. 6 indexed citations
14.
Sessarego, Mario, et al.. (1989). Cytogenetic follow-up after bone marrow transplantation for Philadelphia-positive chronic myeloid leukemia. Cancer Genetics and Cytogenetics. 42(2). 253–261. 12 indexed citations
15.
Sessarego, Mario, Raffaella Defferrari, Anna Dejana, et al.. (1989). Cytogenetic analysis in essential thrombocythemia at diagnosis and at transformation. Cancer Genetics and Cytogenetics. 43(1). 57–65. 50 indexed citations
16.
Sessarego, Mario, Cristina Mareni, R. Vimercati, et al.. (1989). Translocation t(9;9)(p13;q34) in Philadelphia-negative chronic myeloid leukemia with breakpoint cluster region rearrangement. Cancer Genetics and Cytogenetics. 43(1). 51–56. 3 indexed citations
17.
Mareni, Cristina, et al.. (1989). Molecular analysis of Philadelphia-negative myeloproliferative syndromes with i(17q). Cancer Genetics and Cytogenetics. 43(2). 195–201. 4 indexed citations
18.
Ajmar, F., et al.. (1983). Fibroblastoid Colony-Forming Cells in Myeloproliferative Disorders. Acta Haematologica. 70(6). 349–356. 6 indexed citations
19.
Ghio, Riccardo, Giovanna Bianchi, Bob Löwenberg, Dicke Ka, & F. Ajmar. (1977). Effects of fibroblasts on the growth of erythroid progenitor cells in vitro.. PubMed. 5(5). 341–7. 19 indexed citations
20.
Tizianello, A, I Pannacciulli, E Salvidio, & F. Ajmar. (1961). A Quantitative Evaluation of the Splenic and Hepatic Share in Normal Hemocatheresis. Acta Medica Scandinavica. 169(3). 303–311. 2 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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